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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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FOX IV — 7 UDI-DI variants, MDR (A.R.C. Laser GmbH)

MD Atlas
A.R.C. Laser GmbH

Data from EUDAMED, last updated May 23, 2026

FOX IV

426015559FOXIV9R

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: A.R.C. Laser GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426015559FOXIV9R
Device name: FOX IV
Device model: LS03500
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: A.R.C. Laser GmbH
SRN: DE-MF-000009383
Country: Germany
Email: info@arclaser.de

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HME3SBVBT07TWAXWS5FPC6F6

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

LS03500-BWAA04260155593239
LS03500-AWAA04260155593215
LS03500-AABB04260155593260
LS03500-GWAA04260155593192
LS03500-BWAB04260155593222
LS03500-AWAB04260155593208
LS03500-GWAB04260155593185